Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 89141974 | HCID 89141974 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90418906 | HCID 90418906 | — |
Reaction Steps
To CH2Cl2 (20 mL) at 0° C. was added 1M solution of diethylzinc in hexane (11.75 mL, 11.75 mmol), followed by dropwise addition of a solution of trifluoroacetic acid (0.6 mL, 7.83 mmol) in CH2Cl2 (8 mL). After stirring for 15 min, a solution of diiodomethane (0.65 mL, 7.83 mmol) in CH2Cl2 (8 mL) was added. The mixture was stirred for 15 min and a clear solution resulted. tert-Butyl 4-hydroxy-4-(2-methylallyl)piperidine-1-carboxylate (12B) (1 g, 3.92 mmol) was added and the mixture was stirred at room temperature overnight. After quenching with 0.1 M aqueous HCl (50 mL), the CH2Cl2 layer was separated, washed with brine, dried (Na2SO4) and concentrated to give the crude product, which was used directly for the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108921B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-0ed1c6911b554637b48f7bf9c3e29791 |
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| Source note | uspto-grants-2015_08 |
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